HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694398Generated: October 26, 2026
Pyrrolidine → 1-(4-Bromo-2-fluorobenzyl)pyrrolidine
https://huagongshe.com/reaction/1694398
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 4-Bromo-2-fluorobenzyl bromide | HCID 2733660 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(4-Bromo-2-fluorobenzyl)pyrrolidine | HCID 22266723 | 90% |
Reaction Steps
A 4-L RB flask, equipped a magnetic stirring bar was charged with pyrrolidine (363 g, 426 mL, 5.1 mol) and acetonitrile (2750 mL). The mixture was cooled with an ice bath to 10° C., then solid 4-bromo-2-fluorobenzylbromide (MATRIX, Cat. #: 1707, 375 g, 1.4 mol) was added in 6 portions, keeping temperature below 20° C. The mixture was stirred at RT for 4 h. The solvent was removed under vacuum. Then 2 L of sat. Na2CO3 aq. and 500 mL of water was added, and the mixture was extracted with DCM (3×700 mL). The extract was dried over Na2SO4 and evaporated. The resulting light yellow oil was distilled under vacuum (˜1 mm, bp. 125° C.) to give 324.5 g (90%) of the product as a colorless oil. LCMS (M+H): 258.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158673B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-5d89c8324c174b509384eb152e3c9d57 |
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| Source note | uspto-grants-2012_04 |
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